Clinical Research Associate II - Site Monitoring & Protocols
Allen Spolden
A leading clinical research organization in New York is looking for a Clinical Research Associate to provide support for clinical trials. The role involves assisting with protocol design, site evaluations, and ongoing study monitoring. Candidates should have a BA, BS, RN, BSN or equivalent, along with 1-2 years of clinical research experience. Strong attention to detail and excellent communication skills are essential. This position offers a chance to be part of impactful clinical studies. #J-18808-Ljbffr
- ...Syneos Health is looking for a Clinical Research Associate II (CRA II) in the United States. This role involves performing site qualification, site initiation, monitoring activities, and ensuring regulatory compliance. The ideal candidate will have a Bachelor's degree...Website
- ...A leading clinical research organization is seeking a CRA II to manage study sites and ensure compliance with protocols. Responsibilities include overseeing patient safety, conducting site visits, and preparing monitoring reports. The ideal candidate will have a minimum...WebsiteNight shift
$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global... ...closely with investigative sites to ensure high-quality trial... ...Perform routine and close-out monitoring visits to ensure studies are... ..., completeness, and protocol adherence. Provide guidance...WebsitePermanent employmentRemote work$91.34k - $114.17k
...CRA II - Adverum East ICON plc is a world... ...intelligence and clinical research organization. We’... ...Clinical Research Associate to join our diverse... ...Doing Conducting site qualification, initiation, monitoring, and close-out visits... ...trials. Ensuring protocol compliance, data...WebsiteFlexible hours- ...Clinical Research Associate I/II Benefits include: Medical, Dental, and Vision Insurance... ...in-house and field monitoring to be considered for this... ...managing and monitoring study sites, maintaining regulatory compliance... ...monitor for adherence to protocol and GCP. In tandem with...WebsiteLocal areaRemote workWorldwide
$91.34k - $114.17k
CRA II - Adverum East ICON plc is a... ...intelligence and clinical research organization. We’re... ...Clinical Research Associate to join our diverse... ...doing Conducting site qualification, initiation, monitoring, and close-out... ...trials. Ensuring protocol compliance, data integrity...WebsiteWork experience placementFlexible hours$91.5k - $137.3k
...Overview The CRA II is a seasoned, experienced... ...professional in monitoring and site management. Responsibilities... ...-site monitoring of clinical research studies as well as... ...site such as protocol deviation/violations... ...Verifies issues or risks associated with blinded or...WebsiteContract workLocal areaRemote workNight shift$70.1k - $126.1k
...Health Commercial LLC is looking for a CRA II - Sponsor Dedicated. This remote position requires managing clinical trial sites, ensuring compliance with regulations and protocol. Responsibilities include site qualification, monitoring, and communicating with study site...WebsiteRemote workFlexible hours- ...ABBVIE is seeking a Clinical Research Associate to oversee clinical trials in the... ...engaging with investigative sites, training staff, and ensuring compliance with study protocols. Qualified candidates will... ...year of clinical research monitoring experience. AbbVie offers a...Website
- ...ProTrials Research, Inc. is seeking a Contract Senior Clinical Research Associate to oversee clinical trial monitoring and management. This role involves ensuring compliance with protocols and SOPs while managing site personnel training and documentation. The ideal candidate...WebsiteContract work
- ...ICON Strategic Solutions is looking for a Clinical Research Associate who will lead clinical trial monitoring with a focus on quality and continuous improvement... .... The individual will ensure adherence to protocols and conduct site visits to support successful trial...Website
- ...A prominent clinical research organization in Philadelphia is seeking a Clinical Research support staff member to assist with clinical... ...research experience. Responsibilities include preparing protocols, monitoring studies, and ensuring compliance with regulations. Strong...Website
- ...025 Industry Pharma/Biotech/Clinical Research Work Experience 1-3 years City... ...design and preparation of protocols and case report forms. Generate... ...of potential clinical sites according to established criteria... .... Conduct ongoing study monitoring, including frequent periodic...WebsiteWork experience placement
- ...Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in... ...project team, sponsor, and the site Build and maintain a good relationship... ...sites on Adverse Events and protocol/process deviations Perform...WebsiteWork visa
$91.5k - $137.3k
...A clinical research organization is seeking a Clinical Research Associate II to oversee study site management in a remote capacity. Ideal candidates will have a degree in a scientific discipline and at least two years of CRA experience, especially in oncology trials....WebsiteRemote work$90k - $140k
...A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA with a focus on Psychiatry or Pain. This remote role involves extensive site monitoring, ensuring adherence to regulations, and engaging in project management activities...WebsiteRemote work- ...Syneos Health is looking for a Single Sponsor CRA I / II to perform site qualification and monitoring activities in the United States. Ideal candidates... ...RN in a related field, along with knowledge of Good Clinical Practice and ICH Guidelines. This role requires up to...Website
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close‑out of assigned clinical trials investigator sites to ensure... ...is responsible for the resolution of all protocol‑related issues for assigned investigator...WebsiteLocal areaRemote work
$115k - $140k
...Fortrea is looking for a Senior Clinical Research Associate (CRA 2) based in New York. This... ...requires 4+ years of Clinical Monitoring experience with a strong emphasis... ...for monitoring clinical trial sites, ensuring compliance with protocols, and reporting any serious...Website$160 - $180 per hour
...Contract Description The Medical Monitor tasks include: Provide clinical development support including Phase... ..., including but not limited to: Protocols, Clinical Study Reports (CSRs)... ...assessments Promptly engage with site staff if/when an SAE arises to ensure...WebsiteHourly payContract workFor contractorsRemote work- Cardiac Monitoring Technician II - Houston Location: Houston, United States Onsite location. Additional location: N/A Role Overview The Cardiac... ...Benefits information available at Boston Scientific benefits site. Equal Employment Opportunity Boston Scientific Corporation...WebsiteWork experience placementWork at officeLocal areaRelocation packageShift workDay shiftWeekday work
- ...estate firm in New York is seeking a Cybersecurity/SOC Analyst II to monitor and analyze threats and incidents to enhance security... ...Competitive compensation and benefits package offered, with a hybrid work model of on-site and remote days. #J-18808-Ljbffr RELATEDWebsiteRemote work
- ...inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance with regulatory standards. Responsibilities include site qualification, monitoring, and documentation as well as acting as a liaison with...WebsiteRemote workFlexible hours
- ...Parexel International is seeking a Senior Clinical Research Associate in Idaho to manage and monitor clinical trial sites. This role ensures compliance with regulatory standards and oversees investigator relationships to promote patient safety and study quality. A Bachelor...Website
- ...inVentiv Health Commercial LLC is seeking an Experienced Clinical Research Associate to perform site management and ensure compliance with regulatory standards. Responsibilities include site qualification, monitoring, and documentation as well as acting as a liaison with...WebsiteRemote jobFlexible hours
$125k - $145k
...Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas... ..., investigational sites, vendors, and Everest... ...clinical trials. Perform protocol/site feasibility and... ...guidelines, monitoring plans, informed consents... ...review/approval of CRA I/II, evaluating their performance...WebsiteContract workTemporary workInterim roleLocal areaRemote work- ...Overview Experienced Clinical Research Associate - Full-Service Syneos... ...Responsibilities Performs site qualification, site initiation, interim monitoring, site management... ...Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses... ...Late Phase, the CRA II will use the business...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Syneos Health is seeking a CRA II based in São Paulo. This role involves performing site qualification, initiation, and management activities to ensure compliance... ...candidate will leverage their knowledge of Good Clinical Practice and manage site-related activities while...Website
$100k - $125k
...Yoh Services LLC is looking for a Clinical Research Associate for a remote, full-time position. The role requires a background... ...of CRA experience. You'll be responsible for monitoring clinical sites, ensuring compliance with protocols, and training site staff. Benefits include...WebsiteFull timeRemote work$105k - $117k
...A leading clinical outsourcing company seeks an Experienced Ophthalmology & Gen Med CRA 2 to join... ...Outsourcing team. This role involves extensive site monitoring, collaboration with study teams, and ensuring patient protocol compliance. Candidates should have a degree in...WebsiteRemote work
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